DE1188801B - Stabilisieren von Polyvinylfluorid - Google Patents
Stabilisieren von PolyvinylfluoridInfo
- Publication number
- DE1188801B DE1188801B DEP27620A DEP0027620A DE1188801B DE 1188801 B DE1188801 B DE 1188801B DE P27620 A DEP27620 A DE P27620A DE P0027620 A DEP0027620 A DE P0027620A DE 1188801 B DE1188801 B DE 1188801B
- Authority
- DE
- Germany
- Prior art keywords
- hydroxy
- phenyl
- benzotriazole
- polyvinyl fluoride
- light
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 229920002620 polyvinyl fluoride Polymers 0.000 title claims description 17
- 230000000087 stabilizing effect Effects 0.000 title description 2
- -1 1,1,3,3 - tetramethylbutyl Chemical group 0.000 claims description 14
- 150000003852 triazoles Chemical class 0.000 claims description 9
- 239000012964 benzotriazole Substances 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 238000000034 method Methods 0.000 claims description 2
- 230000006641 stabilisation Effects 0.000 claims description 2
- 238000011105 stabilization Methods 0.000 claims description 2
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 16
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 16
- 229920000642 polymer Polymers 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 5
- 238000000465 moulding Methods 0.000 description 5
- 230000015556 catabolic process Effects 0.000 description 3
- 238000006731 degradation reaction Methods 0.000 description 3
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 2
- 239000006096 absorbing agent Substances 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 150000001565 benzotriazoles Chemical class 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 230000002035 prolonged effect Effects 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- IYAZLDLPUNDVAG-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4-(2,4,4-trimethylpentan-2-yl)phenol Chemical compound CC(C)(C)CC(C)(C)C1=CC=C(O)C(N2N=C3C=CC=CC3=N2)=C1 IYAZLDLPUNDVAG-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 206010073306 Exposure to radiation Diseases 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- CIZVQWNPBGYCGK-UHFFFAOYSA-N benzenediazonium Chemical compound N#[N+]C1=CC=CC=C1 CIZVQWNPBGYCGK-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- MCPKSFINULVDNX-UHFFFAOYSA-N drometrizole Chemical compound CC1=CC=C(O)C(N2N=C3C=CC=CC3=N2)=C1 MCPKSFINULVDNX-UHFFFAOYSA-N 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000000320 mechanical mixture Substances 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 230000003313 weakening effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3472—Five-membered rings
- C08K5/3475—Five-membered rings condensed with carbocyclic rings
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US46065A US3018269A (en) | 1960-07-29 | 1960-07-29 | Polymeric compositions, shaped articles therefrom and process of preparation |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1188801B true DE1188801B (de) | 1965-03-11 |
Family
ID=21941400
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DEP27620A Pending DE1188801B (de) | 1960-07-29 | 1961-07-28 | Stabilisieren von Polyvinylfluorid |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US3018269A (enrdf_load_stackoverflow) |
| BE (1) | BE606676A (enrdf_load_stackoverflow) |
| DE (1) | DE1188801B (enrdf_load_stackoverflow) |
| FR (1) | FR1296243A (enrdf_load_stackoverflow) |
| GB (1) | GB919069A (enrdf_load_stackoverflow) |
| NL (1) | NL267656A (enrdf_load_stackoverflow) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3239483A (en) * | 1960-08-08 | 1966-03-08 | Exxon Research Engineering Co | Stabilization of polyisobutylene polymers with sulfur and benzotriazoles |
| NL272014A (enrdf_load_stackoverflow) * | 1960-12-01 | |||
| BE623419A (enrdf_load_stackoverflow) * | 1961-10-10 | |||
| US3230194A (en) * | 1961-12-22 | 1966-01-18 | American Cyanamid Co | 2-(2'-hydroxy-5'-tertiary-octylphenyl)-benzotriazole and polyolefins stabilized therewith |
| US3223496A (en) * | 1962-07-05 | 1965-12-14 | Sinclair Research Inc | Light stabilized hydrocarbon fuel |
| US3282886A (en) * | 1962-07-27 | 1966-11-01 | Du Pont | Polycarbonamides of improved photostability and dye lightfastness |
| US3282842A (en) * | 1964-03-06 | 1966-11-01 | Mobil Oil Corp | Lubricating oil compositions |
| US3983132A (en) * | 1974-08-23 | 1976-09-28 | Gaf Corporation | Branched chain dodecyl isomeric mixtures of 2-(5-dodecyl-2-hydroxy phenyl) benzotriazole as stabilizers for heat and light sensitive materials |
| US4275004A (en) * | 1978-06-26 | 1981-06-23 | Ciba-Geigy Corporation | High caustic coupling process for preparing substituted 2-nitro-2'-hydroxyazobenzenes |
| US4347180A (en) * | 1979-05-16 | 1982-08-31 | Ciba-Geigy Corporation | High caustic coupling process for preparing substituted 2-nitro-2'-hydroxyazobenzenes |
| JPS59215378A (ja) * | 1983-05-21 | 1984-12-05 | Konishiroku Photo Ind Co Ltd | 乳化分散物 |
| US4870121A (en) * | 1987-10-26 | 1989-09-26 | Canadian Patents & Development Ltd. | Electrical tree suppression in high-voltage polymeric insulation |
| US5254608A (en) * | 1989-10-19 | 1993-10-19 | E. I. Du Pont De Nemours And Company | Ultraviolet screener blends |
| US6251173B1 (en) | 1999-10-29 | 2001-06-26 | Lexmark International, Inc. | Ink compositions containing ultraviolet absorbers |
| US7572461B2 (en) * | 2004-03-05 | 2009-08-11 | Kenneth I. Sawyer | Borer-resistant wood, wood products, and wooden structures and methods |
| CA2566605A1 (en) | 2004-05-14 | 2005-12-01 | Kenneth I. Sawyer | Polyurea compositions and compounds for the preparation thereof |
-
0
- NL NL267656D patent/NL267656A/xx unknown
- BE BE606676D patent/BE606676A/xx unknown
-
1960
- 1960-07-29 US US46065A patent/US3018269A/en not_active Expired - Lifetime
-
1961
- 1961-07-21 GB GB26620/61A patent/GB919069A/en not_active Expired
- 1961-07-26 FR FR869124A patent/FR1296243A/fr not_active Expired
- 1961-07-28 DE DEP27620A patent/DE1188801B/de active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| GB919069A (en) | 1963-02-20 |
| BE606676A (enrdf_load_stackoverflow) | |
| FR1296243A (fr) | 1962-06-15 |
| NL267656A (enrdf_load_stackoverflow) | |
| US3018269A (en) | 1962-01-23 |
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